Primary disruption of the default mode network subsystems in drug-naïve Parkinson’s disease with mild cognitive impairments
Purpose Mild cognitive impairment (MCI) in Parkinson’s disease (PD) is related to the disrupted connectivity in networks involved in cognition, primarily in the default mode network (DMN). The DMN contains a midline core and two distinct subsystems (dorsal medial prefrontal cortex (DMPFC) and medial...
Gespeichert in:
Veröffentlicht in: | Neuroradiology 2020-06, Vol.62 (6), p.685-692 |
---|---|
Hauptverfasser: | , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 692 |
---|---|
container_issue | 6 |
container_start_page | 685 |
container_title | Neuroradiology |
container_volume | 62 |
creator | Hou, Yanbing Yuan, Xiaoqin Wei, Qianqian Ou, Ruwei Yang, Jing Gong, Qiyong Shang, Huifang |
description | Purpose
Mild cognitive impairment (MCI) in Parkinson’s disease (PD) is related to the disrupted connectivity in networks involved in cognition, primarily in the default mode network (DMN). The DMN contains a midline core and two distinct subsystems (dorsal medial prefrontal cortex (DMPFC) and medial temporal lobe (MTL) subsystems).
Methods
The strength of functional connectivity (FCS) in intra- and inter-subsystems of DMN and the regional FCS were compared between any two groups from 28 drug-naïve PD patients with MCI (PD-MCI), 19 drug-naïve PD patients with cognitive unimpaired (PD-CU), and 28 age- and sex-matched healthy controls (HCs) by using the nonparametric permutation method (10,000 permutations) with age, sex, and education as covariates and False Discovery Rate (FDR) correction.
Results
For intra-subsystems, the decreased FCS was only detected in the DMPFC subsystem of PD-MCI patients compared with HCs. For inter-subsystems, PD-MCI patients displayed decreased FCS between the posterior cingulate cortex (PCC) and DMPFC subsystem compared with HCs. Furthermore, the temporal parietal junction (TPJ) in the DMPFC subsystem showed decreased regional FCS in the PD-MCI subgroup relative to the HC group. No significant change of FCS was found between PD-MCI and PD-CU patients, and between PD-CU patients and HCs. The sum of FCS values within the DMPFC subsystem and FCS values between the PCC and DMPFC subsystem had a significant power to distinguish PD-MCI patients from PD-CU patients (area under curve (AUC) = 0.703).
Conclusion
The DMPFC subsystem was predominantly disrupted in the PD-MCI subgroup and may have the potential to discriminate PD with MCI. |
doi_str_mv | 10.1007/s00234-020-02378-z |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2356605576</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2405800972</sourcerecordid><originalsourceid>FETCH-LOGICAL-c375t-f60a249fa2b519d4114f254dfacd4df9c0284af904ba24d4337d48e3b4a050663</originalsourceid><addsrcrecordid>eNp9kU9u1TAQhy0Eoq-FC7BAlth0Ezrxn-RliSqgSJXaBawtJ7Zf3Sb2w-O0ahcV1-AUHIKbcBL8SAGJBQvbi_nmN7Y_Ql7U8LoGaI8QgHFRAYOyeLuu7h6RVS04q-qOwWOyKvV1xTsBe2Qf8RIAeMvbp2SPM2iEbLoVuT9PftLplhqPad5mHwONjuYLS411eh4znaKxNNh8E9MVxbnHW8x2QuoDNWneVEF__3Zt6blOVz5gDD--fMVdnNVo6Y3PF3Tyo6FD3ASffSH9tNU-TTZkfEaeOD2iff5wHpBP795-PD6pTs_efzh-c1oNvJW5cg1oJjqnWS_rzoi6Fo5JYZweTNm7oTxUaNeB6AtnBOetEWvLe6FBQtPwA3K45G5T_DxbzGryONhx1MHGGRXjsmlAynaHvvoHvYxzCuV2igmQa4CuZYViCzWkiJisU9vlI1UNamdHLXZUsaN-2VF3penlQ_TcT9b8afmtowB8AbCUwsamv7P_E_sT2K-euQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2405800972</pqid></control><display><type>article</type><title>Primary disruption of the default mode network subsystems in drug-naïve Parkinson’s disease with mild cognitive impairments</title><source>MEDLINE</source><source>SpringerLink Journals</source><creator>Hou, Yanbing ; Yuan, Xiaoqin ; Wei, Qianqian ; Ou, Ruwei ; Yang, Jing ; Gong, Qiyong ; Shang, Huifang</creator><creatorcontrib>Hou, Yanbing ; Yuan, Xiaoqin ; Wei, Qianqian ; Ou, Ruwei ; Yang, Jing ; Gong, Qiyong ; Shang, Huifang</creatorcontrib><description>Purpose
Mild cognitive impairment (MCI) in Parkinson’s disease (PD) is related to the disrupted connectivity in networks involved in cognition, primarily in the default mode network (DMN). The DMN contains a midline core and two distinct subsystems (dorsal medial prefrontal cortex (DMPFC) and medial temporal lobe (MTL) subsystems).
Methods
The strength of functional connectivity (FCS) in intra- and inter-subsystems of DMN and the regional FCS were compared between any two groups from 28 drug-naïve PD patients with MCI (PD-MCI), 19 drug-naïve PD patients with cognitive unimpaired (PD-CU), and 28 age- and sex-matched healthy controls (HCs) by using the nonparametric permutation method (10,000 permutations) with age, sex, and education as covariates and False Discovery Rate (FDR) correction.
Results
For intra-subsystems, the decreased FCS was only detected in the DMPFC subsystem of PD-MCI patients compared with HCs. For inter-subsystems, PD-MCI patients displayed decreased FCS between the posterior cingulate cortex (PCC) and DMPFC subsystem compared with HCs. Furthermore, the temporal parietal junction (TPJ) in the DMPFC subsystem showed decreased regional FCS in the PD-MCI subgroup relative to the HC group. No significant change of FCS was found between PD-MCI and PD-CU patients, and between PD-CU patients and HCs. The sum of FCS values within the DMPFC subsystem and FCS values between the PCC and DMPFC subsystem had a significant power to distinguish PD-MCI patients from PD-CU patients (area under curve (AUC) = 0.703).
Conclusion
The DMPFC subsystem was predominantly disrupted in the PD-MCI subgroup and may have the potential to discriminate PD with MCI.</description><identifier>ISSN: 0028-3940</identifier><identifier>EISSN: 1432-1920</identifier><identifier>DOI: 10.1007/s00234-020-02378-z</identifier><identifier>PMID: 32064569</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Case-Control Studies ; Cognition ; Cognitive ability ; Cognitive Dysfunction - complications ; Cognitive Dysfunction - diagnostic imaging ; Cortex (cingulate) ; Default Mode Network - diagnostic imaging ; Female ; Functional Neuroradiology ; Humans ; Image Interpretation, Computer-Assisted ; Imaging ; Magnetic Resonance Imaging - methods ; Male ; Medicine ; Medicine & Public Health ; Middle Aged ; Movement disorders ; Neurodegenerative diseases ; Neurology ; Neuroradiology ; Neurosciences ; Neurosurgery ; Parkinson Disease - complications ; Parkinson Disease - diagnostic imaging ; Parkinson's disease ; Permutations ; Prefrontal cortex ; Prefrontal Cortex - diagnostic imaging ; Radiology ; Sex ; Subgroups ; Subsystems ; Temporal cortex ; Temporal lobe ; Temporal Lobe - diagnostic imaging</subject><ispartof>Neuroradiology, 2020-06, Vol.62 (6), p.685-692</ispartof><rights>Springer-Verlag GmbH Germany, part of Springer Nature 2020</rights><rights>Springer-Verlag GmbH Germany, part of Springer Nature 2020.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-f60a249fa2b519d4114f254dfacd4df9c0284af904ba24d4337d48e3b4a050663</citedby><cites>FETCH-LOGICAL-c375t-f60a249fa2b519d4114f254dfacd4df9c0284af904ba24d4337d48e3b4a050663</cites><orcidid>0000-0003-0947-1151</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s00234-020-02378-z$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s00234-020-02378-z$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,41464,42533,51294</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32064569$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hou, Yanbing</creatorcontrib><creatorcontrib>Yuan, Xiaoqin</creatorcontrib><creatorcontrib>Wei, Qianqian</creatorcontrib><creatorcontrib>Ou, Ruwei</creatorcontrib><creatorcontrib>Yang, Jing</creatorcontrib><creatorcontrib>Gong, Qiyong</creatorcontrib><creatorcontrib>Shang, Huifang</creatorcontrib><title>Primary disruption of the default mode network subsystems in drug-naïve Parkinson’s disease with mild cognitive impairments</title><title>Neuroradiology</title><addtitle>Neuroradiology</addtitle><addtitle>Neuroradiology</addtitle><description>Purpose
Mild cognitive impairment (MCI) in Parkinson’s disease (PD) is related to the disrupted connectivity in networks involved in cognition, primarily in the default mode network (DMN). The DMN contains a midline core and two distinct subsystems (dorsal medial prefrontal cortex (DMPFC) and medial temporal lobe (MTL) subsystems).
Methods
The strength of functional connectivity (FCS) in intra- and inter-subsystems of DMN and the regional FCS were compared between any two groups from 28 drug-naïve PD patients with MCI (PD-MCI), 19 drug-naïve PD patients with cognitive unimpaired (PD-CU), and 28 age- and sex-matched healthy controls (HCs) by using the nonparametric permutation method (10,000 permutations) with age, sex, and education as covariates and False Discovery Rate (FDR) correction.
Results
For intra-subsystems, the decreased FCS was only detected in the DMPFC subsystem of PD-MCI patients compared with HCs. For inter-subsystems, PD-MCI patients displayed decreased FCS between the posterior cingulate cortex (PCC) and DMPFC subsystem compared with HCs. Furthermore, the temporal parietal junction (TPJ) in the DMPFC subsystem showed decreased regional FCS in the PD-MCI subgroup relative to the HC group. No significant change of FCS was found between PD-MCI and PD-CU patients, and between PD-CU patients and HCs. The sum of FCS values within the DMPFC subsystem and FCS values between the PCC and DMPFC subsystem had a significant power to distinguish PD-MCI patients from PD-CU patients (area under curve (AUC) = 0.703).
Conclusion
The DMPFC subsystem was predominantly disrupted in the PD-MCI subgroup and may have the potential to discriminate PD with MCI.</description><subject>Case-Control Studies</subject><subject>Cognition</subject><subject>Cognitive ability</subject><subject>Cognitive Dysfunction - complications</subject><subject>Cognitive Dysfunction - diagnostic imaging</subject><subject>Cortex (cingulate)</subject><subject>Default Mode Network - diagnostic imaging</subject><subject>Female</subject><subject>Functional Neuroradiology</subject><subject>Humans</subject><subject>Image Interpretation, Computer-Assisted</subject><subject>Imaging</subject><subject>Magnetic Resonance Imaging - methods</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Middle Aged</subject><subject>Movement disorders</subject><subject>Neurodegenerative diseases</subject><subject>Neurology</subject><subject>Neuroradiology</subject><subject>Neurosciences</subject><subject>Neurosurgery</subject><subject>Parkinson Disease - complications</subject><subject>Parkinson Disease - diagnostic imaging</subject><subject>Parkinson's disease</subject><subject>Permutations</subject><subject>Prefrontal cortex</subject><subject>Prefrontal Cortex - diagnostic imaging</subject><subject>Radiology</subject><subject>Sex</subject><subject>Subgroups</subject><subject>Subsystems</subject><subject>Temporal cortex</subject><subject>Temporal lobe</subject><subject>Temporal Lobe - diagnostic imaging</subject><issn>0028-3940</issn><issn>1432-1920</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>BENPR</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNp9kU9u1TAQhy0Eoq-FC7BAlth0Ezrxn-RliSqgSJXaBawtJ7Zf3Sb2w-O0ahcV1-AUHIKbcBL8SAGJBQvbi_nmN7Y_Ql7U8LoGaI8QgHFRAYOyeLuu7h6RVS04q-qOwWOyKvV1xTsBe2Qf8RIAeMvbp2SPM2iEbLoVuT9PftLplhqPad5mHwONjuYLS411eh4znaKxNNh8E9MVxbnHW8x2QuoDNWneVEF__3Zt6blOVz5gDD--fMVdnNVo6Y3PF3Tyo6FD3ASffSH9tNU-TTZkfEaeOD2iff5wHpBP795-PD6pTs_efzh-c1oNvJW5cg1oJjqnWS_rzoi6Fo5JYZweTNm7oTxUaNeB6AtnBOetEWvLe6FBQtPwA3K45G5T_DxbzGryONhx1MHGGRXjsmlAynaHvvoHvYxzCuV2igmQa4CuZYViCzWkiJisU9vlI1UNamdHLXZUsaN-2VF3penlQ_TcT9b8afmtowB8AbCUwsamv7P_E_sT2K-euQ</recordid><startdate>20200601</startdate><enddate>20200601</enddate><creator>Hou, Yanbing</creator><creator>Yuan, Xiaoqin</creator><creator>Wei, Qianqian</creator><creator>Ou, Ruwei</creator><creator>Yang, Jing</creator><creator>Gong, Qiyong</creator><creator>Shang, Huifang</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QO</scope><scope>7RV</scope><scope>7TK</scope><scope>7U7</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M7P</scope><scope>MBDVC</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-0947-1151</orcidid></search><sort><creationdate>20200601</creationdate><title>Primary disruption of the default mode network subsystems in drug-naïve Parkinson’s disease with mild cognitive impairments</title><author>Hou, Yanbing ; Yuan, Xiaoqin ; Wei, Qianqian ; Ou, Ruwei ; Yang, Jing ; Gong, Qiyong ; Shang, Huifang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c375t-f60a249fa2b519d4114f254dfacd4df9c0284af904ba24d4337d48e3b4a050663</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Case-Control Studies</topic><topic>Cognition</topic><topic>Cognitive ability</topic><topic>Cognitive Dysfunction - complications</topic><topic>Cognitive Dysfunction - diagnostic imaging</topic><topic>Cortex (cingulate)</topic><topic>Default Mode Network - diagnostic imaging</topic><topic>Female</topic><topic>Functional Neuroradiology</topic><topic>Humans</topic><topic>Image Interpretation, Computer-Assisted</topic><topic>Imaging</topic><topic>Magnetic Resonance Imaging - methods</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Middle Aged</topic><topic>Movement disorders</topic><topic>Neurodegenerative diseases</topic><topic>Neurology</topic><topic>Neuroradiology</topic><topic>Neurosciences</topic><topic>Neurosurgery</topic><topic>Parkinson Disease - complications</topic><topic>Parkinson Disease - diagnostic imaging</topic><topic>Parkinson's disease</topic><topic>Permutations</topic><topic>Prefrontal cortex</topic><topic>Prefrontal Cortex - diagnostic imaging</topic><topic>Radiology</topic><topic>Sex</topic><topic>Subgroups</topic><topic>Subsystems</topic><topic>Temporal cortex</topic><topic>Temporal lobe</topic><topic>Temporal Lobe - diagnostic imaging</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hou, Yanbing</creatorcontrib><creatorcontrib>Yuan, Xiaoqin</creatorcontrib><creatorcontrib>Wei, Qianqian</creatorcontrib><creatorcontrib>Ou, Ruwei</creatorcontrib><creatorcontrib>Yang, Jing</creatorcontrib><creatorcontrib>Gong, Qiyong</creatorcontrib><creatorcontrib>Shang, Huifang</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Biotechnology Research Abstracts</collection><collection>Proquest Nursing & Allied Health Source</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>Advanced Technologies & Aerospace Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Research Library</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Nursing & Allied Health Premium</collection><collection>Advanced Technologies & Aerospace Database</collection><collection>ProQuest Advanced Technologies & Aerospace Collection</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><jtitle>Neuroradiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hou, Yanbing</au><au>Yuan, Xiaoqin</au><au>Wei, Qianqian</au><au>Ou, Ruwei</au><au>Yang, Jing</au><au>Gong, Qiyong</au><au>Shang, Huifang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Primary disruption of the default mode network subsystems in drug-naïve Parkinson’s disease with mild cognitive impairments</atitle><jtitle>Neuroradiology</jtitle><stitle>Neuroradiology</stitle><addtitle>Neuroradiology</addtitle><date>2020-06-01</date><risdate>2020</risdate><volume>62</volume><issue>6</issue><spage>685</spage><epage>692</epage><pages>685-692</pages><issn>0028-3940</issn><eissn>1432-1920</eissn><abstract>Purpose
Mild cognitive impairment (MCI) in Parkinson’s disease (PD) is related to the disrupted connectivity in networks involved in cognition, primarily in the default mode network (DMN). The DMN contains a midline core and two distinct subsystems (dorsal medial prefrontal cortex (DMPFC) and medial temporal lobe (MTL) subsystems).
Methods
The strength of functional connectivity (FCS) in intra- and inter-subsystems of DMN and the regional FCS were compared between any two groups from 28 drug-naïve PD patients with MCI (PD-MCI), 19 drug-naïve PD patients with cognitive unimpaired (PD-CU), and 28 age- and sex-matched healthy controls (HCs) by using the nonparametric permutation method (10,000 permutations) with age, sex, and education as covariates and False Discovery Rate (FDR) correction.
Results
For intra-subsystems, the decreased FCS was only detected in the DMPFC subsystem of PD-MCI patients compared with HCs. For inter-subsystems, PD-MCI patients displayed decreased FCS between the posterior cingulate cortex (PCC) and DMPFC subsystem compared with HCs. Furthermore, the temporal parietal junction (TPJ) in the DMPFC subsystem showed decreased regional FCS in the PD-MCI subgroup relative to the HC group. No significant change of FCS was found between PD-MCI and PD-CU patients, and between PD-CU patients and HCs. The sum of FCS values within the DMPFC subsystem and FCS values between the PCC and DMPFC subsystem had a significant power to distinguish PD-MCI patients from PD-CU patients (area under curve (AUC) = 0.703).
Conclusion
The DMPFC subsystem was predominantly disrupted in the PD-MCI subgroup and may have the potential to discriminate PD with MCI.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>32064569</pmid><doi>10.1007/s00234-020-02378-z</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0003-0947-1151</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0028-3940 |
ispartof | Neuroradiology, 2020-06, Vol.62 (6), p.685-692 |
issn | 0028-3940 1432-1920 |
language | eng |
recordid | cdi_proquest_miscellaneous_2356605576 |
source | MEDLINE; SpringerLink Journals |
subjects | Case-Control Studies Cognition Cognitive ability Cognitive Dysfunction - complications Cognitive Dysfunction - diagnostic imaging Cortex (cingulate) Default Mode Network - diagnostic imaging Female Functional Neuroradiology Humans Image Interpretation, Computer-Assisted Imaging Magnetic Resonance Imaging - methods Male Medicine Medicine & Public Health Middle Aged Movement disorders Neurodegenerative diseases Neurology Neuroradiology Neurosciences Neurosurgery Parkinson Disease - complications Parkinson Disease - diagnostic imaging Parkinson's disease Permutations Prefrontal cortex Prefrontal Cortex - diagnostic imaging Radiology Sex Subgroups Subsystems Temporal cortex Temporal lobe Temporal Lobe - diagnostic imaging |
title | Primary disruption of the default mode network subsystems in drug-naïve Parkinson’s disease with mild cognitive impairments |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-28T23%3A30%3A38IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Primary%20disruption%20of%20the%20default%20mode%20network%20subsystems%20in%20drug-na%C3%AFve%20Parkinson%E2%80%99s%20disease%20with%20mild%20cognitive%20impairments&rft.jtitle=Neuroradiology&rft.au=Hou,%20Yanbing&rft.date=2020-06-01&rft.volume=62&rft.issue=6&rft.spage=685&rft.epage=692&rft.pages=685-692&rft.issn=0028-3940&rft.eissn=1432-1920&rft_id=info:doi/10.1007/s00234-020-02378-z&rft_dat=%3Cproquest_cross%3E2405800972%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2405800972&rft_id=info:pmid/32064569&rfr_iscdi=true |